東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Macrocyclic host-guest framework for...

Liu, Xianzhi.

FindBook

Google Book

Amazon

博客來

Macrocyclic host-guest framework for polymerization of diiodobutadiyne.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Macrocyclic host-guest framework for polymerization of diiodobutadiyne./
作者:	Liu, Xianzhi.
面頁冊數:	73 p.
附註:	Source: Masters Abstracts International, Volume: 52-03.
Contained By:	Masters Abstracts International52-03(E).
標題:	Chemistry, General. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1546692
ISBN:	9781303465642

Macrocyclic host-guest framework for polymerization of diiodobutadiyne.
Liu, Xianzhi.

Macrocyclic host-guest framework for polymerization of diiodobutadiyne. - 73 p.

Source: Masters Abstracts International, Volume: 52-03.

Thesis (M.S.)--State University of New York at Stony Brook, 2013.

Conjugated organic polymers have optical and electronic properties that make them candidates for applications in organic field effect transistors (OFETs) and light emitting materials. Polydiacetylenes (PDAs) are an important branch of conjugated polymers with alternating poly(ene-yne) structure. The all-carbon polymer without any side groups is carbyne, which has only alternating single and triple carbon-carbon bonds. Carbyne provides a good opportunity to investigate the inherent properties of conjugated polymers. Polydiiododiacetylene (PIDA), a simple PDA with only iodine atom substituents, can be successfully obtained by the topochemical polymerization of the monomer diiodobutadiyne. This polymerization is achieved through the use of bis(nitrile) or bis(pyridyl) hosts, which hold the monomer in the correct orientation for polymerization by a halogen bond between the Lewis-basic nitrogen and the Lewis-acidic iodine. With the goal of forming carbyne, PIDA has been partially dehalogenated by Lewis bases such as pyrollidine, however, inter-and intramolecular aggregation prevented full dehalogenation. In this project, an innovative macrocyclic host-guest framework was designed and evaluated for the preparation of PIDA. The macrocyclic host has the function of keeping individual PIDA strands separate and elongated so that Lewis bases can access all the iodine. The macrocyclic host should be able to self-assemble into a tubular framework with enough inner space to accommodate the monomer, diiodobutadiyne. This host should also possess a nitrogen group that can weakly interact with the monomer to hold it in place. Finally, the host should have solubility commensurate with the monomer, since co-crystallization is carried out by slow evaporation. Several possible designs were proposed and computational modeling was performed to analyze the relation between conformation and ring size, as well as whether or not there is a need for a rigidity-increasing segment and a solubility-increasing segment. Based on the evaluation, the target molecule was selected for synthesis. Several steps have been optimized in the synthesis of the macrocyclic host, including hydroxylation and PEG-tosylation of 2,6-dibromopyridine, followed by a Sonogashira coupling with an alkyne-functionalized phthalimide group. Hydrazinolysis was attempted on a model compound and the host precursor to convert the phthalimide group into the amine. Several other detour routes were considered, including Boc protection on the amine before Sonogashira coupling.

ISBN: 9781303465642Subjects--Topical Terms:

1021807
Chemistry, General.

Macrocyclic host-guest framework for polymerization of diiodobutadiyne.
LDR:03417nam a2200277 4500 001 1960697
005 20140624205951.5
008 150210s2013 ||||||||||||||||| ||eng d
020 $a 9781303465642
035 $a (MiAaPQ)AAI1546692
035 $a AAI1546692
040 $a MiAaPQ $c MiAaPQ
100 1 $a Liu, Xianzhi. $3 2096403
245 1 0 $a Macrocyclic host-guest framework for polymerization of diiodobutadiyne.
300 $a 73 p.
500 $a Source: Masters Abstracts International, Volume: 52-03.
500 $a Adviser: Nancy S. Goroff.
502 $a Thesis (M.S.)--State University of New York at Stony Brook, 2013.
520 $a Conjugated organic polymers have optical and electronic properties that make them candidates for applications in organic field effect transistors (OFETs) and light emitting materials. Polydiacetylenes (PDAs) are an important branch of conjugated polymers with alternating poly(ene-yne) structure. The all-carbon polymer without any side groups is carbyne, which has only alternating single and triple carbon-carbon bonds. Carbyne provides a good opportunity to investigate the inherent properties of conjugated polymers. Polydiiododiacetylene (PIDA), a simple PDA with only iodine atom substituents, can be successfully obtained by the topochemical polymerization of the monomer diiodobutadiyne. This polymerization is achieved through the use of bis(nitrile) or bis(pyridyl) hosts, which hold the monomer in the correct orientation for polymerization by a halogen bond between the Lewis-basic nitrogen and the Lewis-acidic iodine. With the goal of forming carbyne, PIDA has been partially dehalogenated by Lewis bases such as pyrollidine, however, inter-and intramolecular aggregation prevented full dehalogenation. In this project, an innovative macrocyclic host-guest framework was designed and evaluated for the preparation of PIDA. The macrocyclic host has the function of keeping individual PIDA strands separate and elongated so that Lewis bases can access all the iodine. The macrocyclic host should be able to self-assemble into a tubular framework with enough inner space to accommodate the monomer, diiodobutadiyne. This host should also possess a nitrogen group that can weakly interact with the monomer to hold it in place. Finally, the host should have solubility commensurate with the monomer, since co-crystallization is carried out by slow evaporation. Several possible designs were proposed and computational modeling was performed to analyze the relation between conformation and ring size, as well as whether or not there is a need for a rigidity-increasing segment and a solubility-increasing segment. Based on the evaluation, the target molecule was selected for synthesis. Several steps have been optimized in the synthesis of the macrocyclic host, including hydroxylation and PEG-tosylation of 2,6-dibromopyridine, followed by a Sonogashira coupling with an alkyne-functionalized phthalimide group. Hydrazinolysis was attempted on a model compound and the host precursor to convert the phthalimide group into the amine. Several other detour routes were considered, including Boc protection on the amine before Sonogashira coupling.
590 $a School code: 0771.
650 4 $a Chemistry, General. $3 1021807
650 4 $a Chemistry, Polymer. $3 1018428
690 $a 0485
690 $a 0495
710 2 $a State University of New York at Stony Brook. $b Chemistry. $3 2094227
773 0 $t Masters Abstracts International $g 52-03(E).
790 $a 0771
791 $a M.S.
792 $a 2013
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1546692